Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Landrieu

Showing results (91-100 of 126) with videos related to

Pageof 13
Sort By:
Revue Neurologique|June 20, 2002
[SPECT-identified hypoperfusion of the left temporomesial structures in a Kleine-Levin syndrome]P Portilla, E Durand, A Chalvon, et al.
Acta Neurochirurgica|January 1, 1989
Vein of Galen aneurysmal malformations. Report of 36 cases managed between 1982 and 1988P Lasjaunias, G Rodesch, K Terbrugge, et al.
Archives of Disease in Childhood|February 6, 2002
Critical illness neuromuscular disease: clinical, electrophysiological, and prognostic aspectsB Tabarki, A Coffiniéres, P Van Den Bergh, et al.
Intensive Care Medicine|May 6, 1999
Haemorrhagic shock and encephalopathy syndrome: neurological course and predictors of outcomeB Thébaud, B Husson, Y Navelet, et al.
European Journal of Pediatrics|August 1, 1990
Varicella-associated pancytopeniaB Bader-Meunier, A Dusser, J M Mersh, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 12, 2000
[Epilepsy presenting as life-threatening events in infants]L Heissessen, A Dusser, V Nouirygat, et al.
The Journal of Pediatrics|November 5, 1997
Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndromeT Ferlin, P Landrieu, C Rambaud, et al.
Archives Francaises De Pediatrie|December 1, 1987
[Prognostic factors in cerebral hypoxic-ischemias in infants less than a year old]M Tardieu, D Devictor, C Wood, et al.
Archives Francaises De Pediatrie|November 1, 1990
[Prognostic evaluation of severe head injuries in children]C Jeannin, E Straub, D Devictor, et al.
Human Molecular Genetics|November 16, 2001
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptorN Monnier, N B Romero, J Lerale, et al.
Pageof 13

Showing results (91-100 of 126) with videos related to

Sort By:
Pageof 13
Revue Neurologique|June 20, 2002
[SPECT-identified hypoperfusion of the left temporomesial structures in a Kleine-Levin syndrome]P Portilla, E Durand, A Chalvon, et al.
Acta Neurochirurgica|January 1, 1989
Vein of Galen aneurysmal malformations. Report of 36 cases managed between 1982 and 1988P Lasjaunias, G Rodesch, K Terbrugge, et al.
Archives of Disease in Childhood|February 6, 2002
Critical illness neuromuscular disease: clinical, electrophysiological, and prognostic aspectsB Tabarki, A Coffiniéres, P Van Den Bergh, et al.
Intensive Care Medicine|May 6, 1999
Haemorrhagic shock and encephalopathy syndrome: neurological course and predictors of outcomeB Thébaud, B Husson, Y Navelet, et al.
European Journal of Pediatrics|August 1, 1990
Varicella-associated pancytopeniaB Bader-Meunier, A Dusser, J M Mersh, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 12, 2000
[Epilepsy presenting as life-threatening events in infants]L Heissessen, A Dusser, V Nouirygat, et al.
The Journal of Pediatrics|November 5, 1997
Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndromeT Ferlin, P Landrieu, C Rambaud, et al.
Archives Francaises De Pediatrie|December 1, 1987
[Prognostic factors in cerebral hypoxic-ischemias in infants less than a year old]M Tardieu, D Devictor, C Wood, et al.
Archives Francaises De Pediatrie|November 1, 1990
[Prognostic evaluation of severe head injuries in children]C Jeannin, E Straub, D Devictor, et al.
Human Molecular Genetics|November 16, 2001
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptorN Monnier, N B Romero, J Lerale, et al.
Pageof 13